CUL4A

Cullin 4A Q13619 CUL4A_HUMAN
Protein Coding Chr 13 13q34 Swiss-Prot reviewed Entrez 8451
Mutations
1,263
CL 124 · Tissue 1,107
Samples
270
CL 39 · Tissue 222
Peptides
225
unique mutant peptides
Transcripts
6
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations1,2631241,107
Samples27039222
Peptides22531190

Function

CUL4A · Cullin 4A

CUL4A is the ubiquitin ligase component of a multimeric complex involved in the degradation of DNA damage-response proteins (Liu et al., 2009 [PubMed 19481525]).[supplied by OMIM, Oct 2009].

Isoforms & Proteins

6 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000375440 Q13619 277 208
ENST00000375441 Q13619-2 236 184
ENST00000326335 A0A0A0MR50* 235 183
ENST00000451881 Q13619-2 234 182
ENST00000617546 Q13619-2 234 182
ENST00000488558 A0A087WWN2* 47 35

Gene Properties

Type
Protein Coding
Chromosome
13
Cytoband
13q34
Entrez ID

Recurrent Mutations

All 208 amino-acid changes on canonical ENST00000375440 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in CUL4A · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in CUL4A – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
Endometrial Carcinoma
2/42 5%
17/612 3%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
6/210 3%
29/1899 2%
Cervical Carcinoma
1/35 3%
6/422 1%
Bladder Carcinoma
0/58 0%
14/956 1%
Neuroendocrine Tumour
4/154 3%
4/577 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Gastric Carcinoma
0/74 0%
17/1809 1%
Colorectal Carcinoma
5/143 4%
25/3239 1%
Other Solid Cancers
2/94 2%
12/1515 1%
Non-Small Cell Lung Carcinoma
5/304 2%
9/1390 1%
Thyroid Gland Carcinoma
0/45 0%
13/1592 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Ovarian Carcinoma
2/109 2%
6/998 1%
Other Sarcomas
0/69 0%
5/699 1%
Non-Cancerous
0/104 0%
6/830 1%
Biliary Tract Carcinoma
0/54 0%
6/950 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
15/2550 1%
Breast Carcinoma
4/144 3%
12/3264 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Glioma
2/52 4%
5/2127 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Pancreatic Carcinoma
3/89 3%
0/1611 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Other Blood Cancers
0/61 0%
3/2725 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Prostate Carcinoma
0/13 0%
1/2105 0%

Mutation Distribution

Where CUL4A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CUL4A were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 1,263 mutations in CUL4A

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide